FDA Inspection 1098613 — Patheon Austria GmbH & Co. KG
The FDA completed an inspection of Patheon Austria GmbH & Co. KG on Nov 30, 2018 in Linz. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 30, 2018
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Linz (Austria)
Additional Details
Mutual Recognition Agreement (MRA)